Treat time matters: Untimely sugar consumption implicated in long-term energy imbalance

IF 5.6 2区 医学 Q1 PHYSIOLOGY Acta Physiologica Pub Date : 2023-10-11 DOI:10.1111/apha.14051
Kristin Eckel-Mahan
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Though light is a primary entrainment cue for the master pacemaker of the brain, the suprachiasmatic nucleus (SCN) of the hypothalamus, food is an important <i>Zeitgeber</i> (or “time-giver”) for many peripheral organs,<span><sup>1</sup></span> where the circadian phase can adapt to the timing of energy intake, as opposed to adhering to the circadian organization provided by the SCN's entrainment to the light/dark cycle. 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Abstract

When to eat your sweet treat? A new study published in this issue by Muguerza et al. suggests that appropriately timed consumption of our favorite confectionaries may be important for long-term energy balance and preservation of our internal 24-h rhythms. The circadian (i.e., 24-h) clock plays a critical role across tissues of the body, where it intricately controls the temporal patterns of gene expression required to maintain important diurnal function within individual cells, and ultimately within individual organs. Though light is a primary entrainment cue for the master pacemaker of the brain, the suprachiasmatic nucleus (SCN) of the hypothalamus, food is an important Zeitgeber (or “time-giver”) for many peripheral organs,1 where the circadian phase can adapt to the timing of energy intake, as opposed to adhering to the circadian organization provided by the SCN's entrainment to the light/dark cycle. Interestingly, a “misalignment” of the circadian clock across peripheral organs and the SCN is thought to be induced by mistimed energy intake patterns,1 and is deleterious for metabolic health in humans and other organisms.2 Both the timing of food intake and the quality of nutrient intake are important for maintaining temporal organization within the body and for driving normal patterns of circadian gene expression.3

In this issue, Muguerza et al. use nocturnal rats to test several metabolic and circadian effects of elevated sugar consumption (“sweet treats”) administered at activity onset (8 p.m., or Zeitgeber time ZT12) versus the onset of the rest phase (8 a.m, ZT0). Though the sweet treat dose was provided by syringe in the form of diluted sweetened condensed milk, equating to only a half teaspoon of sugar for human consumption, time of day of administration had a profound effect on several metabolic and circadian properties. First, consistent with a body of literature showing time-of-day effects of energy intake on body weight (reviewed in4), rats administered the excess sugar at rest onset ultimately gained more weight compared to rats who consumed the sweet treat at the activity onset, despite no changes in overall energy intake (Figure 1).

Importantly, while energy intake was not different between groups, rhythmicity of glucose was maintained only in the rats consuming the excess sugar at the activity onset. Interestingly, insulin rhythmicity was preserved in both groups, though rhythmic patterns were antiphase in the two feeding groups. Insulin signaling results in direct modification of proteins involved in the central transcriptional translational feedback loop of the circadian clock,5 suggesting possible uncoupling or misalignment of the circadian clock in vivo depending on the time at which the sweet treat was administered. Notably, the diurnal timing of sugar administration altered the circadian rhythms of several core clock genes in the hypothalamus, and a considerably lower number of serum metabolites (several of which are involved in energy metabolism) were rhythmic in the rats consuming the sweet treat at the onset of rest phase compared to the onset of the active phase.

One asset of the study design included the experimenters controlling for movement and possible changes in stress hormones when rats were perturbed by humans. For example, all rats were housed in the same room and required to approach the end of the cage at the save Zeitgeber time, regardless of whether or not they consumed the treat. Several important considerations should be reflected on, however. For example, what was a sweet treat for the rats would likely have a marginal impact on insulin secretion for most humans, where the sugar content of most foods is already considerably high. For example, in the United States, one of the countries with the highest sugar consumption in the world, an average individual consumes approximately 34 teaspoons of sugar a day according to the United States Department of Agriculture (https://www.ars.usda.gov/). This is probably not surprising, considering that an average sugary drink has in the range of 7–12 teaspoons of sugar per serving. In this study, rats were provided the sweet treat on a backdrop of vivarium chow diet, which consisted of 3.2% sugar, roughly one fifth of the percent consumed by an average adult in the United States. Still, considering the high sugar content of many snacks consumed worldwide, the study results can be extrapolated to the eating habits and patterns of humans, and the deleterious effects that timing can have on metabolism and energy balance.

Circadian disruption is associated with metabolic disease, including obesity and diabetes.6 In this context, time-restricted eating can be considered a form of circadian medicine, wherein timed application of intervention (in this case energy intake) can be used to target and exploit the circadian clock.7 The quote by Hippocrates, “Let food by thy medicine and medicine by thy food,” is often cited to emphasize the powerful impact of nutrition on health. Increasingly understood is the extent to which the timing of energy intake may be important for delaying metabolic disease and its progression. This study underscores that even the timing of snacks with sufficient calories to alter insulin secretion and blood glucose may be important for maintaining energy balance in the long term.

Kristin Eckel-Mahan: wrote the article.

The author declared no conflict of interest.

Kristin Eckel-Mahan is funded by NIH grants DK114037 and DK125922.

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治疗时间很重要:摄入过量的糖会导致长期的能量失衡。
什么时候吃甜食?Muguerza等人在本期发表的一项新研究表明,适当定时食用我们最喜欢的糖果可能对长期能量平衡和保持我们的24小时内在节奏很重要。昼夜节律(即24小时)时钟在身体各组织中发挥着关键作用,它复杂地控制着维持单个细胞内以及最终在单个器官内重要的昼夜功能所需的基因表达的时间模式。尽管光是大脑主要起搏器(下丘脑的视交叉上核(SCN))的主要夹带线索,但食物是许多外周器官的重要时代信使(或“时间给予者”),1在这些器官中,昼夜节律可以适应能量摄入的时间,而不是坚持SCN对光/暗周期的夹带所提供的昼夜节律组织。有趣的是,外周器官和SCN的昼夜节律时钟“错位”被认为是由不合时宜的能量摄入模式引起的,1并且对人类和其他生物体的代谢健康有害。2食物摄入的时间和营养摄入的质量对于维持体内的时间组织和驱动昼夜节律基因表达的正常模式都很重要。3在这个问题上,Muguerza等人使用夜间活动的大鼠来测试在活动开始时(晚上8点,或Zeitgeber时间ZT12)服用的高糖(“甜食”)与休息阶段开始时(上午8点,ZT0)的几种代谢和昼夜节律影响。尽管甜味剂是通过注射器以稀释的加糖炼乳的形式提供的,相当于人类食用的半茶匙糖,但一天中的给药时间对几种代谢和昼夜节律特性有着深远的影响。首先,与大量显示能量摄入对体重影响的文献一致(见4),尽管总能量摄入没有变化,但与在活动开始时摄入甜食的大鼠相比,在休息开始时摄入过量糖的大鼠最终增加了更多的体重(图1)。重要的是,虽然各组之间的能量摄入没有差异,但只有在活动开始时摄入过量糖的大鼠才能维持葡萄糖的节律性。有趣的是,尽管两个喂养组的节律模式相反,但两组的胰岛素节律性都得到了保留。胰岛素信号传导导致参与昼夜节律时钟的中央转录-翻译反馈环的蛋白质的直接修饰,5这表明体内昼夜节律时钟可能解耦或错位,这取决于给予甜食的时间。值得注意的是,糖给药的昼夜节律改变了下丘脑中几个核心时钟基因的昼夜节律,与活动期开始相比,在休息期开始时摄入甜食的大鼠中,血清代谢产物(其中几个与能量代谢有关)的节律性要低得多。研究设计的一项资产包括实验者在大鼠受到人类干扰时控制运动和应激激素的可能变化。例如,所有大鼠都被安置在同一个房间里,并被要求在节省Zeitgeber时间接近笼子的末端,无论它们是否食用了这种食物。然而,应当考虑到几个重要的考虑因素。例如,对大鼠来说,甜食可能会对大多数人的胰岛素分泌产生轻微影响,因为大多数食物的含糖量已经相当高。例如,根据美国农业部的数据,在世界上糖消费量最高的国家之一美国,平均每人每天消耗约34茶匙糖(https://www.ars.usda.gov/)。考虑到每份含糖饮料的平均含糖量在7-12茶匙之间,这可能并不奇怪。在这项研究中,大鼠在间日粮的背景下吃甜食,间日粮由3.2%的糖组成,大约是美国成年人平均摄入量的五分之一。尽管如此,考虑到世界各地食用的许多零食含糖量很高,研究结果可以推断出人类的饮食习惯和模式,以及时间对新陈代谢和能量平衡的有害影响。昼夜节律紊乱与代谢疾病有关,包括肥胖和糖尿病。6在这种情况下,限时进食可以被视为昼夜节律医学的一种形式,其中定时应用干预(在本例中为能量摄入)可以用于靶向和利用昼夜节律钟。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Physiologica
Acta Physiologica 医学-生理学
CiteScore
11.80
自引率
15.90%
发文量
182
审稿时长
4-8 weeks
期刊介绍: Acta Physiologica is an important forum for the publication of high quality original research in physiology and related areas by authors from all over the world. Acta Physiologica is a leading journal in human/translational physiology while promoting all aspects of the science of physiology. The journal publishes full length original articles on important new observations as well as reviews and commentaries.
期刊最新文献
Correction to "Beneficial effects of MGL-3196 and BAM15 combination in a mouse model of fatty liver disease". Issue Information Impaired suppression of fatty acid release by insulin is a strong predictor of reduced whole-body insulin-mediated glucose uptake and skeletal muscle insulin receptor activation. Differential production of mitochondrial reactive oxygen species between mouse (Mus musculus) and crucian carp (Carassius carassius) A quantitative analysis of bestrophin 1 cellular localization in mouse cerebral cortex.
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